Autoantibodies and other tests in rheum Flashcards

1
Q

Scl-70 (anti-topoisomerase)

A

40% of diffuse scleroderma
15% limited
- higher risk of ILD

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2
Q

RNA polymerase III

A

17% in scleroderma

  • increased risk of renal crisis
  • increased risk of malignancy
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3
Q

anti-centromere antibodies

A

80% of limited scleroderma (CREST)

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4
Q

Anti-Jo-1

A

Polymyositis

Anti-Synthetase syndrome

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5
Q

Anti-Mi2

A

Dermatomyositis

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6
Q

Pattern of ANA seen in limited systemic sclerosis?

A

Centromere

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7
Q

Pattern of ANA seen in diffuse systemic sclerosis?

A

Speckled

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8
Q

Pattern of ANA seen in poly/dermatomyositis?

A

Speckled

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9
Q

Pattern of ANA seen in sjogrens?

A

Speckled

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10
Q

Pattern of ANA seen in lupus?

A

Homogeneous and rim pattern most specific

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11
Q

Anti-ds DNA

A

SLE

  • highly specific but only 70% sensitive
  • only 70% of patients with SLE have positive dsDNA
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12
Q

Anti-histone antibodies

A

SLE

- often indicate drug induced lupus

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13
Q

ANA pattern in RA

A

Homogeneous

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14
Q

Most common and least specific ANA pattern

A

Speckled

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15
Q

What tests are useful for monitoring SLE?

A

Anti dsDNA

Complement, ESR, renal function, urinalysis for protein

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16
Q

What is considered a high titre ANA?

A

1:640

17
Q

Rheumatoid factor?

A

Rheumatoid arthritis
As sensitive as anti-CCP (around 70%) but less specific
Can be positive in:
Sjogrens
SLE
Hepatitis C, sarcoid, infective endocarditis, cryoglobulinemia

18
Q

Anti-CCP?

A

Specific for RA (more specific then RF but same sensitivity)

Predicts more erosive and more severe disease

19
Q

Anti-Ro/La

A

Sjogrens syndrome (70% sensitivity)
SLE (30% sensitivity)
- in SLE predicts higher rate of neonatal lupus (rash and complete heart block)
- women with anti-Ro antibody, carry a 3% chance of having a baby with neonatal lupus

20
Q

cANCA

A

anti-neutrophil antibody against proteinase-3

Granulomatosis with polyangiitis (90% sensitivity when disease is active, not used for monitoring)

21
Q

pANCA

A

anti-neutrophil antibody against myeloperoxidase
microscopic polyangiitis - 80% sensitivity
churg strauss - 60% sensitivity
* note atypical pANCA (not MPO) can be seen in inflammatory bowel disease

22
Q

Type 1 cryoglobulins

A

Monoclonal IgM or IgG

  • caused by lymphoproliferative disorders Waldenstroms, MM, lymphoma
  • not particulary good at activating complement so do not become clinically apparent until high enough to cause hyperviscosity
23
Q

Type 2 cryoglobulins

A

Monoclonal RF (usually IgM or IgA) against the Fc portion of IgG

  • most associated with hep C and HIV
  • most common type
24
Q

Type 3 cryoglobulins

A

Polyclonal RF against IgG

- most associated with underlying connective tissue disorders

25
Q

What is meant by mixed cryoglobulinemia?

A

Type 2 and 3

- types that involve RF

26
Q

What is a cryoglobulin?

A

Immunoglobulins that precipitate in the cold and dissolve on re-warming

27
Q

Complement levels in mixed cryoglobulinemia?

A

Low C4 and normal C3

28
Q

Complement levels in a lupus flare?

A

Low C3 and C4

  • activation of classical pathway = both low
  • activation of alternative pathway = low C3 and normal C4
29
Q

Complement findings in post strep GN?

A

Low C3 and normal C4